ID: ALA4470357

Max Phase: Preclinical

Molecular Formula: C33H42Br2N6O4

Molecular Weight: 586.74

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1cc(C[N+](C)(C)CC#CCOC2=NOCC2)ccc1/N=N/c1ccc(C[N+](C)(C)CC#CCOC2=NOCC2)cc1.[Br-].[Br-]

Standard InChI:  InChI=1S/C33H42N6O4.2BrH/c1-27-24-29(26-39(4,5)19-7-9-21-41-33-17-23-43-37-33)12-15-31(27)35-34-30-13-10-28(11-14-30)25-38(2,3)18-6-8-20-40-32-16-22-42-36-32;;/h10-15,24H,16-23,25-26H2,1-5H3;2*1H/q+2;;/p-2/b35-34+;;

Standard InChI Key:  PHHDJUCTVRTJND-KGNAMTJXSA-L

Associated Targets(Human)

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Chrm1 Muscarinic acetylcholine receptor (3770 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 586.74Molecular Weight (Monoisotopic): 586.3257AlogP: 5.07#Rotatable Bonds: 10
Polar Surface Area: 86.36Molecular Species: NEUTRALHBA: 8HBD: 0
#RO5 Violations: 2HBA (Lipinski): 10HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: 13.66CX Basic pKa: 0.95CX LogP: -2.51CX LogD: -2.51
Aromatic Rings: 2Heavy Atoms: 43QED Weighted: 0.22Np Likeness Score: -0.33

References

1. Agnetta L, Bermudez M, Riefolo F, Matera C, Claro E, Messerer R, Littmann T, Wolber G, Holzgrabe U, Decker M..  (2019)  Fluorination of Photoswitchable Muscarinic Agonists Tunes Receptor Pharmacology and Photochromic Properties.,  62  (6): [PMID:30827105] [10.1021/acs.jmedchem.8b01822]

Source